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1.
Bull Cancer ; 107(12): 1241-1251, 2020 Dec.
Article in French | MEDLINE | ID: mdl-33092818

ABSTRACT

INTRODUCTION: End-of-life platelet transfusion practice in onco-hematology is subjective and depends on representations shared by patients, nurses and hematologists. This study aims to describe these representations of platelet transfusion in a context of a severe and advanced hematologic malignancy through the social representation of its protagonists. METHODS: A qualitative study, using the associative network method and including three groups of 15 participants (patients with an advanced hematologic malignancy, regularly transfused in platelet concentrates; nurses and hematologic oncologists) from four hematology centers was conducted between February and April 2019. Analysis was carried out using IraMuTeQ software. RESULTS: Patients expect platelet transfusion to have a direct beneficial impact on their health and highlight human relations. Nurses aim at the patient's well-being, in his or her individuality, and at respecting the transfusion protocol. Physicians seek to relieve symptoms by taking into account a multitude of decision-making factors. The textual clustering method, nuances those previous results and individualizes four different orientations, independent of groups: dependency, singularity, subjectivity and neutrality. DISCUSSION: The perception of the social representations related to platelet transfusion at the end-of-life should make it possible to adapt the discourse to the preferred orientation of the speaker and could be an asset in goals of care discussion with patients as well as with teams in charge of palliative care.


Subject(s)
Hematologic Neoplasms/psychology , Medical Staff, Hospital/psychology , Nursing Staff, Hospital/psychology , Platelet Transfusion/psychology , Terminal Care/psychology , Aged , Aged, 80 and over , Decision Making , Hematologic Neoplasms/therapy , Humans , Interpersonal Relations , Middle Aged , Qualitative Research
2.
Arch Cardiovasc Dis ; 112(3): 199-216, 2019 Mar.
Article in English | MEDLINE | ID: mdl-30621917

ABSTRACT

The French Working Group on Perioperative Haemostasis (GIHP) and the French Study Group on Haemostasis and Thrombosis (GFHT), in collaboration with the French Society for Anaesthesia and Intensive Care (SFAR), drafted up-to-date proposals on the management of antiplatelet therapy for non-elective invasive procedures or bleeding complications. The proposals were discussed and validated by a vote; all proposals could be assigned with a high strength. Management of oral antiplatelet agents in emergency settings requires knowledge of their pharmacokinetic and pharmacodynamic parameters, evaluation of the degree of alteration of haemostatic competence and the associated bleeding risk. Platelet function testing may be considered. When antiplatelet agent-induced bleeding risk may worsen the prognosis, measures should be taken to neutralize antiplatelet therapy, by considering not only the efficacy of available means (which can be limited for prasugrel and even more for ticagrelor), but also the risks that these means expose the patient to. The measures include platelet transfusion at the appropriate dose and haemostatic agents (tranexamic acid; recombinant activated factor VII for ticagrelor). When possible, postponing non-elective invasive procedures at least for a few hours until the elimination of the active compound (which could compromise the effect of transfused platelets) or, if possible, for a few days (reduction of the effect of antiplatelet agents) should be considered.


Subject(s)
Blood Loss, Surgical/prevention & control , Perioperative Care/methods , Platelet Aggregation Inhibitors/administration & dosage , Postoperative Hemorrhage/prevention & control , Administration, Oral , Consensus , Drug Administration Schedule , Drug Monitoring/standards , Humans , Platelet Aggregation Inhibitors/adverse effects , Platelet Aggregation Inhibitors/pharmacokinetics , Platelet Function Tests/standards , Platelet Transfusion , Postoperative Hemorrhage/blood , Postoperative Hemorrhage/chemically induced , Risk Assessment , Risk Factors , Societies, Medical/standards , Treatment Outcome
3.
Transfus Clin Biol ; 25(3): 228-235, 2018 Sep.
Article in English | MEDLINE | ID: mdl-30077511

ABSTRACT

Inherited platelet disorders are rare bleeding syndromes due to either platelet function abnormalities or thrombocytopenia which may be associated with functional defects. The haemorrhagic symptoms observed in these patients are mostly muco-cutaneous and of highly variable severity. Although 30 to 50% of the platelet disorders are still of unknown origin, the precise diagnosis of these pathologies by specialized laboratories together with haemorrhagic scores enables an assessment of the risk of bleeding in each patient. Depending on the diagnostic elements collected, an appropriate medical procedure can be proposed for each situation: scheduled or emergency surgical interventions and pregnancy follow-up. The pathologies most at risk correspond to Glanzmann's thrombasthenia, Bernard-Soulier syndrome, severe thrombocytopenia (<40,000 platelets/µL) and signalling protein abnormalities affecting the activation of GPIIb-IIIa, a membrane glycoprotein essential for platelet aggregation. For these particular patients, in whom the risk of bleeding can be increased by a factor of 40, management protocols during surgical procedures are generally based on the use of conventional platelet concentrates, for both prophylaxis and the control of active bleeding. The perinatal period in women with platelet disorders and their new-born also require special attention. Indeed, beyond unpredictable delivery haemorrhages, bleeding requiring a blood transfusion is observed after delivery in more than 50% of women with Glanzmann's thrombastenia or Bernard-Soulier syndrome.


Subject(s)
Blood Platelet Disorders/complications , Blood Platelet Disorders/genetics , Hemorrhage/etiology , Hemorrhage/therapy , Humans , Risk Factors
4.
Transfus Clin Biol ; 24(3): 166-171, 2017 Sep.
Article in French | MEDLINE | ID: mdl-28673503

ABSTRACT

Fetal and neonatal allo-immune thrombocytopenia (FNAIT) is considered as a rare disease due to the incidence (1/1000-1/2000 births). The major complication of severe thrombocytopenia is bleeding and particularly intra-cranial hemorrhage and neurologic sequelae following. Serology and molecular biology developments have reconfigured the platelet immunology diagnosis. Anti-HPA-1a allo-immunisation is responsible for more than 80% FNAIT cases with a high recurrence rate of severe bleeding complications. Therapeutic management has changed over the coming years from an invasive concept associating fetal blood sampling and in utero platelet transfusion to a non invasive treatment by intravenous immunoglobulins injection (IVIg). The purpose of this article is to provide an update on FNAIT management in the light of current developments over the past 30years.


Subject(s)
Blood Platelets/immunology , Thrombocytopenia, Neonatal Alloimmune/therapy , Antigens, Human Platelet/immunology , Blood Transfusion, Intrauterine , Disease Management , Female , Fetal Blood/chemistry , Fetal Diseases/immunology , Fetal Diseases/therapy , Fetal Therapies/methods , Histocompatibility, Maternal-Fetal/immunology , Humans , Immunoglobulins, Intravenous , Infant, Newborn , Intracranial Hemorrhages/etiology , Intracranial Hemorrhages/prevention & control , Isoantibodies/immunology , Male , Practice Guidelines as Topic , Pregnancy , Prenatal Diagnosis , Thrombocytopenia, Neonatal Alloimmune/diagnosis , Thrombocytopenia, Neonatal Alloimmune/embryology , Thrombocytopenia, Neonatal Alloimmune/immunology
5.
Transfus Clin Biol ; 24(3): 101-105, 2017 Sep.
Article in French | MEDLINE | ID: mdl-28709844

ABSTRACT

Principles of transfusion strategy have been used for neonates and children similar to adults. However, due to substantial discrepancies between physiology/pathology in children and in their adult counterparts, decisions, indications, and doses are different from those of adults, especially in neonates. Specific data and practice guidelines for blood product transfusion are reported owing to the experience of pediatrics and neonatology units and partners of the French Blood product bank.


Subject(s)
Blood Transfusion/standards , Neonatology , Pediatrics , Practice Guidelines as Topic , Blood Component Transfusion/standards , Blood Grouping and Crossmatching , Blood Transfusion/legislation & jurisprudence , Blood Transfusion/methods , Child , Child, Preschool , France , Humans , Infant , Infant, Newborn , Parental Consent/legislation & jurisprudence , Transfusion Reaction/prevention & control
6.
Transfus Clin Biol ; 24(3): 160-165, 2017 Sep.
Article in French | MEDLINE | ID: mdl-28645644

ABSTRACT

Antiplatelet agents are at risk for bleeding complications, the management of which differs depending on the clinical situation and on the antiplatelet agent itself. Neutralization of antiplatelets is sometimes necessary, most often leading to platelet transfusion, although the benefit of this strategy is poorly documented. In addition, if platelet transfusion corrects the platelet inhibition induced by aspirin and probably by clopidogrel and prasugrel, it does not neutralize ticagrelor, as a consequence of its pharmacological properties. The clinical benefit of platelet transfusion is limited, and the most recent studies are challenging it. However, it is indicated on a perioperative basis for surgeries with high hemorrhagic risk and is discussed in severe hemorrhages. The neutralization of ticagrelor is a concern and the antidote currently under development may be a solution. In all cases, other therapeutic solutions may be considered, such as administration of desmopressin, tranexamic acid or activated factor VII.


Subject(s)
Hemorrhage/therapy , Platelet Aggregation Inhibitors/adverse effects , Platelet Transfusion , Adenosine/adverse effects , Adenosine/analogs & derivatives , Adenosine/therapeutic use , Antidotes , Aspirin/adverse effects , Aspirin/therapeutic use , Clopidogrel , Hemorrhage/chemically induced , Humans , Platelet Aggregation Inhibitors/therapeutic use , Prasugrel Hydrochloride/adverse effects , Prasugrel Hydrochloride/therapeutic use , Purinergic P2Y Receptor Antagonists/therapeutic use , Risk , Ticagrelor , Ticlopidine/adverse effects , Ticlopidine/analogs & derivatives , Ticlopidine/therapeutic use
7.
Rev Med Interne ; 38(7): 467-473, 2017 Jul.
Article in French | MEDLINE | ID: mdl-28528236

ABSTRACT

Like all antithrombotic drugs, antiplatelet agents expose to a risk of bleeding complications. Clinical research has extensively focused on the efficacy of these drugs to reduce ischemic events. The bleeding risk associated with them was solely considered as an inevitable and acceptable complication. When two new potent P2Y12-receptor inhibitors, prasugrel and ticagrelor, were marketed, the risk of major bleeding increased. These new agents have modified the balance between the absolute risk reduction in ischemic events and the absolute risk increase in bleeding events. This paper is an update on the bleeding risk assessment associated with antiplatelet agents. It discusses the place of platelet function monitoring, and the optimal management of bleeding complications. It addresses the challenging issue of reversal of antiplatelet therapy, focusing especially on ticagrelor, which pharmacodynamics complicate bleeding management.


Subject(s)
Drug-Related Side Effects and Adverse Reactions/therapy , Hemorrhage/chemically induced , Hemorrhage/therapy , Platelet Aggregation Inhibitors/therapeutic use , Adenosine/administration & dosage , Adenosine/adverse effects , Adenosine/analogs & derivatives , Aspirin/administration & dosage , Aspirin/adverse effects , Clopidogrel , Drug-Related Side Effects and Adverse Reactions/prevention & control , Humans , Platelet Aggregation Inhibitors/adverse effects , Risk Factors , Ticagrelor , Ticlopidine/administration & dosage , Ticlopidine/adverse effects , Ticlopidine/analogs & derivatives
8.
Transfus Clin Biol ; 23(4): 217-221, 2016 Nov.
Article in French | MEDLINE | ID: mdl-27592154

ABSTRACT

Neonatal immune thrombocytopenia represent less than 5% of cases of early thrombocytopenia (early-onset<72hours post-delivery). As in adults, thrombocytopenia in neonates is defined as a platelet count less than 150G/L. They are either auto- or allo-immune. Thrombocytopenia resulting from transplacental passage of maternal antibodies directed to platelet membrane glycoproteins can be severe. The major complication of severe thrombocytopenia is bleeding and particularly intra-cranial haemorrhage and neurologic sequelea following. However, auto- and allo-immune thrombocytopenia have very different characteristics including the treatment management. In fact, this treatment is based on platelet transfusion associated or not to intravenous immunoglobulin administration. The purpose of this article is to remind platelet transfusion's place in neonatal immune thrombocytopenia in terms of recently published French guidelines and international practices.


Subject(s)
Platelet Transfusion , Thrombocytopenia, Neonatal Alloimmune/therapy , Combined Modality Therapy , France , Humans , Immunity, Maternally-Acquired , Immunoglobulins, Intravenous , Infant, Newborn , Intracranial Hemorrhages/etiology , Intracranial Hemorrhages/prevention & control , Practice Guidelines as Topic , Purpura, Thrombocytopenic, Idiopathic/complications , Purpura, Thrombocytopenic, Idiopathic/therapy
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